Randomized Study Comparing Metabolic Surgery With Intensive Medical Therapy to Treat Diabetic Kidney Disease (OBESE-DKD)

May 27, 2021 updated by: Ricardo Vitor Cohen, MD, Hospital Alemão Oswaldo Cruz

Open, Randomized, Unicenter Study Comparing Metabolic Surgery With Intensive Medical Therapy to Treat Diabetic Kidney Disease

Proven therapy for DKD is primarily limited to RAAS blockers and SLGT2i. Weight reduction has the potential to become an additional and much needed treatment option. Of all the weight reduction strategies metabolic surgery is suited to be the most effective. Yet no study has of yet compared the effect of metabolic surgery against best medical treatment on the progression of DKD. This pilot trial is designed to be the first determine the efficacy of metabolic surgery in slowing progression of DKD as compared to best medical therapy. The study design will address all the major limitations previously documented, including the major dilemma of estimating versus measuring GFR. Of note, the study's design will allow its sample size to be adjusted upward using an adaptive design if necessary, to achieve statistical significance. It will also inform study design and sample size issues for all future studies in this field. The payoff of establishing metabolic surgery as a new and effective intervention to slow progression to ESRD would be great in terms of reducing patient suffering and societal costs.

This will be an open-label, randomized trial involving sixty (60) patients with diabetic kidney disease (DKD) and obesity who will undergo Roux-en-Y gastric bypass (RYGB) in the intervention arm or receive best medical treatment (BMT) in the control arm.

The aim of this prospective, open, randomized study is to evaluate the efficacy and safety of RYGB surgery versus best medical treatment on the progression of DKD in patients with type 2 diabetes and obesity.

Study Overview

Detailed Description

This will be an open-label, randomized trial involving sixty (60) patients with DKD and obesity who will undergo RYGB (intervention arm) or receive BMT (control arm).

Thirty (30) obese patients with DKD will undergo gastric bypass. Patients will also receive standard of care medical therapy for DKD (ACEI or ARB + SGLT2i) and T2DM (metformin, glitazones, incretin therapy - DPP4 inhibitor and GLP-1 analogs - and insulin, if necessary). Other comorbidities, such as hypertension and dyslipidemia, will be treated according to the latest recommendations of the ADA. The surgical procedure will consist of a laparoscopic surgery performed by an experienced surgeon (approximately 6000 bariatric surgeries), who is accredited as surgeon of excellence by the Brazilian Society of Bariatric and Metabolic Surgery and Surgical Review and Surgical Review Corporation program since 2009.

Thirty (30) obese patients with DKD will undergo best medical treatment for DKD (ACEI or ARB + SGLT2i) and T2DM (metformin, glitazones, incretin therapy - DPP4 inhibitor and GLP-1 analogs - and insulin, if necessary). Other comorbidities, such as hypertension and dyslipidemia, will be treated according to the latest recommendations of the ADA.

Regarding medication therapy: Metformin will be maintained in the postoperative period while fasting glycemia is above 100 mg/dL unless contraindicated. Anti-antihypertensive drugs and medications for dyslipidemia will be maintained in the postoperative period, unless contraindicated. Micronutrient supplementation (vitamins and mineral salts) will be prescribed to all patients undergoing metabolic surgery. Patients allocated to the control group will receive the same supplementation if necessary.

Study Type

Interventional

Enrollment (Anticipated)

60

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • São Paulo
      • Sao Paulo, São Paulo, Brazil, 01323-020
        • Recruiting
        • Centro especializado em Obesidade e Diabetes do Hospital Alemão Oswaldo Cruz
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Female or male aged ≥30 and ≤70 years
  • Diabetic kidney disease as defined by an estimated glomerular filtration rate (eGFR) (as estimated by CKD-EPI creatinine + cystatin C equation)72 between 45-59l/min/1.73m2 and macroalbuminuria (≥ 300 mg/g) in a 24 hr urine sample
  • BMI ≥30-40 kg/m2
  • Fasting C-peptide over 1 ng/ml
  • Negative glutamic acid decarboxylase autoantibodies test
  • Patients having received accurate information about the surgery and requesting the procedure
  • Patients having understood and accepted the need for long-term medical and surgical follow-up
  • Effective method of contraception in women of child-bearing age
  • Signed informed consent document

Exclusion Criteria:

  • Refusal to participate
  • Autoimmune diabetes/type 1 diabetes
  • Previous abdominal operations that would complicate a metabolic surgery or increase surgical risk
  • Previous malabsorptive and restrictive surgeries
  • Malabsorptive syndromes and inflammatory bowel disease
  • Significant and/or severe hepatic disease that may complicate metabolic surgery
  • Pregnancy or women of childbearing age without effective contraceptive
  • Recent history of neoplasia (< 5 years), except for non-melanoma skin neoplasms
  • History of liver cirrhosis, active chronic hepatitis, active hepatitis B or hepatitis C
  • Major cardiovascular event in the last 6 months
  • Current angina
  • Pulmonary embolism or severe thrombophlebitis in the last 2 years
  • Positive HIV serum testing
  • Mental incapacity or severe mental illness
  • Severe psychiatric disorders that would complicate follow-up after randomization
  • Alcoholism or illicit drug use
  • Uncontrolled coagulopathy
  • Participation in other clinical trials in the past 30 days
  • Inability to tolerate RAAS blockers and/or SGLT2i
  • Iodine allergy
  • History of acute kidney injury requiring renal replacement therapy
  • Dialysis dependency
  • Kidney transplantation
  • Use of immunosuppressive drugs, chemotherapy and/or radiotherapy
  • Any disorder which, in the opinion of the investigator, might jeopardize subject's safety or compliance with the protocol

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: RYGB (intervention arm)
Thirty (30) obese patients with DKD will undergo gastric bypass. Patients will also receive standard of care medical therapy for DKD (ACEI or ARB + SGLT2i) and T2DM (metformin, glitazones, incretin therapy - DPP4 inhibitor and GLP-1 analogs - and insulin, if necessary). Other comorbidities, such as hypertension and dyslipidemia, will be treated according to the latest recommendations of the ADA. The surgical procedure will consist of a laparoscopic surgery performed by an experienced surgeon (approximately 6000 bariatric surgeries), who is accredited as surgeon of excellence by the Brazilian Society of Bariatric and Metabolic Surgery and Surgical Review and Surgical Review Corporation program since 2009.
  1. Pneumoperitoneum closed with Veress needle
  2. Identification of Treitz angle
  3. Measurement of biliary loop (50 cm)
  4. Bowel transection with linear stapler (white load)
  5. Measurement of the alimentary limb (100 cm)
  6. Laterolateral Entero-anastomoses (white load)
  7. Construction of gastric pouch distant about 3 cm from the esophageal-gastric junction with stomach section in the small curvature.
  8. Linear cutting anastomosis (gastrojejunostomy) from about 1 to 1.2 cm
  9. Anastomosis integrity evaluation by methylene blue test and/or perioperative air.

Expected surgical time: 60 minutes

Other Names:
  • RYGB
Patients will also receive standard of care medical therapy for DKD (ACEI or ARB + SGLT2i) and T2DM (metformin, glitazones, incretin therapy - DPP4 inhibitor and GLP-1 analogs - and insulin, if necessary).
Other Names:
  • BMT
Active Comparator: BMT (control arm).
Thirty (30) obese patients with DKD will undergo best medical treatment for DKD (ACEI or ARB + SGLT2i) and T2DM (metformin, glitazones, incretin therapy - DPP4 inhibitor and GLP-1 analogs - and insulin, if necessary). Other comorbidities, such as hypertension and dyslipidemia, will be treated according to the latest recommendations of the ADA.
Patients will also receive standard of care medical therapy for DKD (ACEI or ARB + SGLT2i) and T2DM (metformin, glitazones, incretin therapy - DPP4 inhibitor and GLP-1 analogs - and insulin, if necessary).
Other Names:
  • BMT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean differenceGlomerular filtration rate (GFR)
Time Frame: At 12 and 36 months after randomization
Mean difference in GFR between BMT and RYGB at the pre-specified time points of 12 and 36 months after randomization
At 12 and 36 months after randomization

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in twenty-four hour urinary albumin/protein excretion
Time Frame: From baseline to 12 and 36 months
Change in 24h urinary albumin/protein excretion
From baseline to 12 and 36 months
Improvements in micro- or macroalbuminuria
Time Frame: From baseline to 12 and 36 months
Proportion of patients who achieve improvements in micro- or macroalbuminuria from baseline to 12 and 36 months
From baseline to 12 and 36 months
Change in CKD stage and CKD prognostic risk
Time Frame: From baseline to 12 and 36 months
Change in CKD stage and CKD prognostic risk from baseline to month 12 and 36
From baseline to 12 and 36 months
Change in GFR, eGFR and 24 hr creatinine clearance
Time Frame: From baseline to 12 and 36 months
Change in GFR, eGFR and 24 hr creatinine clearance from baseline to months 12 and 36
From baseline to 12 and 36 months
Proportion of participants with ≥30%, ≥40%, and ≥50% reduction in GFR measurements
Time Frame: From baseline to 12 and 36 months
Proportion of participants with ≥30%, ≥40%, and ≥50% reduction in GFR measurements (GFR, eGFR and 24 hr creatinine clearance) from baseline to months 12 and 36
From baseline to 12 and 36 months
Decline in eGFR, sustained low eGFR, kidney transplantation, maintenance dialysis, and kidney death
Time Frame: Time to occurrence (from baseline)
Time to occurrence of sustained % decline in eGFR, sustained low eGFR, kidney transplantation, maintenance dialysis, and kidney death
Time to occurrence (from baseline)
Maintenance dialysis, kidney transplantation, kidney death, and GFR < 15 ml/min
Time Frame: At 12 and 36 months after randomization
Individual and composite endpoints of maintenance dialysis, kidney transplantation, kidney death, and GFR < 15 ml/min at 12 and 36 months
At 12 and 36 months after randomization
Change in body weight
Time Frame: From baseline to 12 and 36 months
Change in body weight from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in body mass index
Time Frame: From baseline to 12 and 36 months
Change in body mass index from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in waist circumference
Time Frame: From baseline to 12 and 36 months
Change in waist circumference from baseline to months 12 and 36
From baseline to 12 and 36 months
Medications to maintain optimal diabetes and blood pressure control
Time Frame: From baseline to 12 and 36 months
Number and dose of medications to maintain optimal diabetes and blood pressure control from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in fasting glucose
Time Frame: From baseline to 12 and 36 months
Change in fasting glucose from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in HbA1c
Time Frame: From baseline to 12 and 36 months
Change in HbA1c from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in basal insulin
Time Frame: From baseline to 12 and 36 months
Change in basal insulin from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in homeostasis model assessment (HOMA) scores
Time Frame: From baseline to 12 and 36 months
Change in homeostasis model assessment (HOMA) scores from baseline to months 12 and 36
From baseline to 12 and 36 months
Remission in type 2 diabetes
Time Frame: At 12 and 36 months after randomization
Achievement of partial or complete remission in type 2 diabetes by months 12 and 36
At 12 and 36 months after randomization
Change in blood pressure
Time Frame: From baseline to 12 and 36 months
Change in blood pressure from baseline to months 12 and 36
From baseline to 12 and 36 months
Hypoglycemic adverse events
Time Frame: From baseline to 12 and 36 months
Number of patients with confirmed or symptomatic hypoglycemic adverse events from baseline to months 12 and 36
From baseline to 12 and 36 months
Changes in total cholesterol, triglycerides, LDL and HDL levels
Time Frame: From baseline to 12 and 36 months
Changes in total cholesterol, triglycerides, LDL and HDL levels from baseline to months 12 and 36
From baseline to 12 and 36 months
Number of participants achieving LDL < 100 mg/dL and HDL > 40mg/dL
Time Frame: From baseline to 12 and 36 months
Number of participants achieving LDL < 100 mg/dL and HDL > 40mg/dL from baseline to months 12 and 36
From baseline to 12 and 36 months
Changes in serum calcium and phosphorus,
Time Frame: From baseline to 12 and 36 months
Changes in serum calcium and phosphorus from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in parathyroid hormone (PTH)
Time Frame: From baseline to 12 and 36 months
Change in parathyroid hormone (PTH) from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in mineral bone density
Time Frame: From baseline to 12 and 36 months
Change in mineral bone density from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in quality of life
Time Frame: From baseline to 12 and 36 months
Change in quality of life measured by SF-36 questionnaire from baseline to months 12 and 36
From baseline to 12 and 36 months
Adverse events
Time Frame: From baseline to 12 and 36 months
Number of patients with adverse events from baseline to months 12 and 36
From baseline to 12 and 36 months
Acute kidney injury
Time Frame: From baseline to 12 and 36 months
Number of episodes of acute kidney injury from baseline to months 12 and 36
From baseline to 12 and 36 months
Adverse cardiovascular events (nonfatal stroke, nonfatal MI, cardiovascular death)
Time Frame: From baseline to 12 and 36 months
Composite of major adverse cardiovascular events (nonfatal stroke, nonfatal MI, cardiovascular death) from baseline to months 12 and 36
From baseline to 12 and 36 months
Mortality
Time Frame: From baseline to 12 and 36 months
Total mortality from baseline to months 12 and 36
From baseline to 12 and 36 months
Days hospitalized
Time Frame: From baseline to 12 and 36 months
Number of days hospitalized from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in urinary volume
Time Frame: From baseline to 12 and 36 months
Change in urinary volume from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in calcium and oxalate excretion
Time Frame: From baseline to 12 and 36 months
Change in calcium and oxalate excretion from baseline to months 12 and 36
From baseline to 12 and 36 months
High sensitivity c-reactive protein
Time Frame: From baseline to 12 and 36 months
Change in high sensitivity c-reactive protein from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in muscle strength
Time Frame: From baseline to 12 and 36 months
Change in muscle strength using one repetition maximum (1-RM) from baseline to months12 and 36
From baseline to 12 and 36 months
Kidney volumes
Time Frame: From baseline to 12 and 36 months
Change in kidney volumes from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in ventricular mass
Time Frame: From baseline to 12 and 36 months
Change in left and right ventricular mass from baseline to months 12 and 36
From baseline to 12 and 36 months
Change in ejection fraction
Time Frame: From baseline to 12 and 36 months
Change in left ventricular ejection fraction from baseline to months 12 and 36
From baseline to 12 and 36 months
Costs of care and health care utilization
Time Frame: From baseline to 12 and 36 months
Costs of care and health care utilization from baseline to months 12 and 36
From baseline to 12 and 36 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ricardo V Cohen, MD, PhD, Oswaldo Cruz German Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 25, 2021

Primary Completion (Anticipated)

December 1, 2024

Study Completion (Anticipated)

December 1, 2024

Study Registration Dates

First Submitted

November 4, 2020

First Submitted That Met QC Criteria

November 10, 2020

First Posted (Actual)

November 12, 2020

Study Record Updates

Last Update Posted (Actual)

May 28, 2021

Last Update Submitted That Met QC Criteria

May 27, 2021

Last Verified

May 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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